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NIH Allocation of ARRA Funds Dollars In BillionsNIH Allocation of ARRA Funds Dollars In Billions
Oversight, Risk ManagementFinancial & Employment Reporting
ARRA appropriated $10 billion directly to NIH
Extramural Repair, Improvements, & Const.
Extramural Scientific Equipment
Intramural Repair, Improvements, & Constr.
Comparative Effectiveness Research
$1.
0
$0.
3$
0.5
AH
RQ
– $
0.4
Extramural Scientific Research(All ICs, OD, Common Fund)
$8.2
ARRA Award FeaturesARRA Award Features ARRA requires recipients to account for, track, monitor, report on, provide
for audit of, and closeout ARRA funding separately from non-ARRA awards
To implement these requirements NIH has established a number of unique business processes
Guide Notice NOT-OD-09-080 Issued 4/3/2009 describing ARRA features:
http://grants.nih.gov/grants/guide/notice-files/NOT-OD-09-080.html
ARRA Award Features: Special TermsARRA Award Features: Special Terms
In addition to the standard NIH terms of award, all NIH ARRA awards will include special ARRA terms
These terms are provided to NIH by HHS
The award includes a link to a PDF attachment posted on the NIH Award Terms website: http://grants.nih.gov/grants/policy/NIH_HHS_ARRA_Award_Terms.pdf
As updates are provided by HHS, they will be posted at this same site.
ARRA Award Features: ARRA Award Features: ARRA Banner, CFDA, CANsARRA Banner, CFDA, CANs
Banner: All ARRA awards will include a banner at the top of each award clearly noting this award as issued under ARRA
CFDAs: NIH has established 2 trans-NIH CFDAs just for ARRA
~ 93.701: For all non-Construction ARRA funding
~ 93.702: For all NCRR Construction ARRA funding
CANs: NIH Institutes/Centers have established unique CANs that are associated with these new CFDAs
Unique Business Processes:Unique Business Processes:Administrative Supplements & Competing RevisionsAdministrative Supplements & Competing Revisions
These present a unique challenge—accommodating the “separation” and accountability required by ARRA while still requiring a programmatic connection to the parent grant
All cumulative references to the parent grant are being removed from ARRA T-3s
ARRA T-3 budget/projects periods will reflect that of the T-3 only and not the parent
Unique Business Processes:Unique Business Processes:Administrative Supplements & Competing Revisions (cont.)Administrative Supplements & Competing Revisions (cont.)
ARRA T-3 budget/project period end dates need not be in “sync” with the parent
ARRA T-3s issued in FY2009 may be for a single budget/project period up to 24 months. Assumes parent record has this time remaining (including any no-cost extension)
ARRA T-3s issued in FY2010 will be no more than a 12-month budget/project period
Unique Business Processes:Unique Business Processes:Administrative Supplements & Competing Revisions (cont.)Administrative Supplements & Competing Revisions (cont.)
No “co-mingling” of ARRA T-3 and parent grant $$$ allowed (assuming parent grant is funded with regular NIH appropriation $$$)
~ Separate institution accounts required
~ Separate PMS drawdowns
~ No rebudgeting between parent and ARRA T-3
~ No carryover of ARRA T-3 balances into the parent
Unique Business Processes:Unique Business Processes:Administrative Supplements & Competing Revisions (cont.)Administrative Supplements & Competing Revisions (cont.)
No-cost Extensions of ARRA-funded T-3s
~ ARRA T-3s are awarded under NIH Terms of Award and will therefore be eligible for a one-time no-cost extension
~ This is separate from the parent record
~ Prior approval requests to extend beyond that initial 12-month extension will only rarely be considered
Unique Business Processes:Unique Business Processes:Administrative Supplements & Competing Revisions (cont.)Administrative Supplements & Competing Revisions (cont.)
Unique Award Terms for ARRA T-3s
~ Will cite standard ARRA Terms
~ Will also include references to separate financial reporting; separate closeout; restrictions on rebudgeting and carryover
Unique Business Processes:Unique Business Processes:Modified Carryover AuthoritiesModified Carryover Authorities
If an ARRA award includes a commitment for an ARRA-funded future year in FY2010, grantees will be able to carryover from the FY2009 budget period into the FY2010 period
No carryover allowed though between ARRA funding budget periods and budget periods funded by non-ARRA fund
Unique Business Processes: Modified Carryover AuthoritiesUnique Business Processes: Modified Carryover Authorities
Grant Number Document Number Notes
5 R01 AI123456-04 RAI123456A Non-ARRA Funded
2 R01 AI123456-05 RAI123456Z ARRA Funded
5 R01 AI123456-06 RAI123456Z ARRA Funded
2 R01 AI123456-07 RAI123456B Non-ARRA Funded
~ 04 Yr funds CANNOT be carried forward into -05; -04 year financially closed
~ 05 Yr funds CAN be carried forward into -06
~ 06 Yr funds CANNOT be carried forward into -07
~ 04 Yr funds CANNOT be carried forward into -07
Unique Funding: 2-Phase RPGUnique Funding: 2-Phase RPG
Some ICs may chose to fund a Research Project Grant (e.g., R01) in 2 phases
~ Phase 1: FY2009 & FY2010 funded with ARRA $$$
~ Phase 2: From the regular IC appropriation beginning in FY2011 or beyond
~ Award for Phase 1 will show only the ARRA project period and future year commitment; the commitments from the regular IC appropriation will be referenced in a special award term
• The Stimulus table has flag settings that will indicate by proposal, by fund whether or not the proposal/fund is Stimulus or non Stimulus.
– These flags are set on the Stimulus table at the proposal level in PDS and at the proposal/fund level in APS
• We can track the following scenarios based on the flag status:
– Stimulus proposal with Stimulus funding: PDS stimulus = Y APS Stimulus = Y– Stimulus proposal with non Stimulus funding: PDS stimulus = Y APS Stimulus = N– Non Stimulus proposal with Stimulus funding: PDS stimulus = N APS Stimulus = Y
• Not included in the Stimulus table– Non Stimulus proposal with non Stimulus funding
• We can track the following scenarios only if the dept admin copies the proposal from the orginal:
– Original Proposal is not stimulus, but the Revised proposal is stimulus and funded or not funded as stimulus.
– Currently, proposals that are marked as Revisions in PDS and have been copied from the original document are tied together thru their proposal ids in PDS.
– This can be seen in the field called Copied From in the PDS application.
– The copied from proposal relationship would provide a good means for Stimulus tracking.
– Revisions that are not tied back to an original document in PDS would require some manual intervention to link them.
Stimulus Pre-Award (PDS) & Post Award (APS)
Tracking Explained
Visual Representation of
Pre-Award (PDS) – Post Award (APS)
TrackingPre-Award
(PDS)
Original Proposal Entered
Post Award (APS)
Stimulus:
Proposal ID: 456
Copied From: 123
Grant Analyst
Revised Proposal Copied
Business Admin
Proposal ID: 789
Copied From:
Revised Proposal
Entered In but not Copied
Proposal ID: 123
Stimulus: X
Stimulus: X
Fund Num: 701-222
Proposal ID: 456
• Proposal id is entered into the APS System upon receiving the award letter.
• Grant Analyst can trace this back to Proposal based on the proposal id from the award letter.
• If revised proposal was copied then it can be traced back to the original proposal
• Once a proposal has been marked as pending or finalized by the Grant Analyst no updates can be made by the business admin.
Trace Back to Proposal
ID
Review Proposals
Enter Award
Stimulus Pre-Award (PDS) & Post Award (APS)
Tracking Recommendation
• It is recommended that proposals not be updated or checked as stimulus because they were awarded stimulus.
– The reason for this is that we have the possibility for revised non-stimulus proposals to be awarded with stimulus funds
– There is a thorough process in place between the business admin and the grant analyst to verify if the proposal should be marked stimulus or not.
– The system prompts the user before saving the proposal to verify if they want the proposal to be marked as stimulus.
• Updates to mark an awarded proposal as stimulus should come only from the central unit and this should be a judgment from the central unit based on accumulated facts from the documentation and conversations with the Dept Admins or PIs
Final NIH Appropriations FY 2009 NIH received $30.4 billion
~ Increase of 3% over FY 2008
~ Supports 9,800 new and competing RPGs
Average competing award expected to increase by 3%
Noncompeting awards to be supported at the most recently committed levels
1% increase in all NRSA stipend levels
More at: http://grants.nih.gov/grants/guide/notice-files/NOT-OD-09-066.html
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Continuing ResolutionContinuing ResolutionImplementation of NIH Fiscal Policy Grant Awards – FY 2009
NOT-OD-09-066
This Notice provides guidance about the NIH Fiscal Operations Plan for FY2009 and it implements the FY 2009 enacted Omnibus appropriation that provided NIH with $ 30.4 billions or 3 percent more than FY 2008 funding. The NIH will continue to manage its portfolio of investments in biomedical research as described in the FY 2008 Fiscal Policy Notice (see http://grants.nih.gov/grants/guide/notice-files/NOT-OD-08-036.html ). This includes continuing to address the need for a highly productive pool of researchers by providing support for new investigators and sustaining established investigators, who have little or no additional research support.
The FY 2009 appropriation allows NIH to support investments in research by funding research grants at the most recently committed levels. Non-competing awards previously issued in FY 2009 at reduced levels (90%) Non-competing awards previously issued in FY 2009 at reduced levels will be revised to restore funds to the level indicated above.
This policy does not apply to Career Awards, SBIR/STTRs, and Ruth L. Kirschstein-National Research Service Award (NRSA) Individual Fellowships & Institutional Training Grants.
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Med School - Continuing Resolution (cont)Med School - Continuing Resolution (cont)SNAP – ModularPDS Document Lump sum, or detailed direct cost budget - Per the Notice of Grant Award (NGA) Recommended Amount (Total Costs), with appropriate F&A rate/sAward Stage Funds will be budgeted according to the Notice of Grant Award (NGA)
SNAP - Non-ModularPDS Document Lump sum, or detailed direct cost budget - Per the NGA Recommended Amount (Total Costs), with appropriate F&A rate/sAward Stage G&C will apply the budgetary cut to either BU 34 or 35 depending on which has the most money
Non-SNAP - Non-ModularPDS Document Full, categorical, detailed budget - Per the NGA Recommended Amount (Total Costs), with appropriate F&A rate/sAward Stage Funds will be budgeted according to the Notice of Grant Award (NGA)
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New Business Process for Submitting Revised Project Summary/Abstracts,New Business Process for Submitting Revised Project Summary/Abstracts, Specific Aims, and/or Public Health Relevance Statements whenSpecific Aims, and/or Public Health Relevance Statements when
Changing the Scope of Proposed Research Projects Changing the Scope of Proposed Research Projects
NOT-OD-09-088Release Date: May 5, 2009Note: Below is Redacted Version of the aforementioned notice. You are responsible for reviewing entire notice Purpose
To advise applicants of a new business process for documenting changes in scope for proposed research projects. These changes can result from applicant discussions with NIH grants management or program staff. For example, some grant applications will require reductions in scope in order to be accomplished in the 2 years or less required by the Recovery Act, thus requiring modifications to the Project Summary/Abstract, Specific Aims, and/or Public Health Relevance sections.
Effective for all Project Summary/Abstract, Specific Aims, and/or Public Health Relevance sections revised after the publication date of this notice, this new business process will facilitate accurate storage of the revised information, and allow the data to be analyzed and accurately reported to the public.
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New Business Process for Submitting Revised Project Summary/Abstracts,New Business Process for Submitting Revised Project Summary/Abstracts, Specific Aims, and/or Public Health Relevance Statements whenSpecific Aims, and/or Public Health Relevance Statements when
Changing the Scope of Proposed Research Projects (cont.)Changing the Scope of Proposed Research Projects (cont.)
Procedure
When requested by NIH, PD/PIs and applicant organization officials should discuss potential changes in scope with NIH Program Officials and revise the Project Summary/Abstract, Specific Aims, and/or Public Health Relevance sections of their application as appropriate. Once all issues are resolved, applicants should e-mail a document with final versions of the revised sections to the IC-designated e-mail as a single Microsoft Word or Adobe PDF file.
All revised application information submitted to the NIH must be approved by an Authorized Organizational Representative (AOR).
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New Business Process for Submitting Revised Project Summary/Abstracts,New Business Process for Submitting Revised Project Summary/Abstracts, Specific Aims, and/or Public Health Relevance Statements whenSpecific Aims, and/or Public Health Relevance Statements when
Changing the Scope of Proposed Research Projects (cont.)Changing the Scope of Proposed Research Projects (cont.)Procedure cont.
The three headings listed below must be included in the document that is submitted even if a particular section had no changes from the previous submission. If there are no changes for a section include the header but leave the text area blank to ensure appropriate processing of this information by NIH’s electronic systems. A template for providing this information can be found at http://grants.nih.gov/grants/funding/424/SF424_RR_Guide_ModifiedScopeTemplate.doc and http://grants.nih.gov/grants/funding/424/SF424_RR_Guide_ModifiedScopeTemplate.pdf.
Modified Project Summary/Abstract SectionProvide a summary of the proposed activity suitable for dissemination to the public. It should be a self-contained description of the project and should contain a statement of objectives and methods to be employed. It should be informative to other persons working in the same or related fields and insofar as possible understandable to a scientifically or technically literate lay reader. This abstract must not include any proprietary or confidential information. This section must be no longer than 30 lines of text.
Modified Specific Aims Section List the broad, long-term objectives and the goal of the specific research proposed, for example, to test a stated hypothesis, create a novel design, solve a specific problem, challenge an existing paradigm or clinical practice, address a critical barrier to progress in the field, or develop new technology. One page is recommended
Modified Public Health Relevance Section Using no more than two or three sentences, describe the relevance of this research to public health. In this section, be succinct and use plain language that can be understood by a general, lay audience.
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Stipend LevelsStipend Levels
Stipend levels have increased please see
NOT-OD-09-075Released: March 27, 2009
RePORT:New Tools to Search NIH Data
Research Portfolio Online Reporting Tool
New reports, data and analyses website released in 2008 and recently significantly expanded with addition of RCDC data (Research, Condition and Disease Categorization process)
Replaces the current Award Information and Data web page and provides:~ Access to Frequently Requested Reports~ FAQs on how success rates are computed~ Information about the NIH budget~ Easy search tools for locating data and reports ~ Links to funding estimates for RCDC data.
More at: http://report.nih.gov
New NIH Policy Limiting Number of ResubmissionNew NIH Policy Limiting Number of Resubmission Recommendation of the Peer Review Oversight Committee:
~ increase the number of high quality and first resubmissions that can be funded earlier
~ reduce applicant burden of multiple resubmissions ~ remove delays in funding for meritorious science.
Number of resubmission applications limited to 1 (original and one resubmission) ~ Applies to all applications submitted for January 25, 2009 due date and beyond. ~ Applications submitted prior to January 25, 2009 are “grandfathered” in and
allowed two resubmissions. Second resubmission must be received by January 7, 2011.
Applies to all activity codes and all applications
More at: http://grants.nih.gov/grants/guide/notice-files/NOT-OD-09-003.html
NIH Priority:NIH Priority: Assistance to Early Stage Investigators Assistance to Early Stage Investigators ESI Definition: A new or first time investigator who is within 10 years of completing
his/her terminal research degree or medical residency (or equivalent).
Identification of ESIs will occur in the Personal Profile section of the eRA Commons. Investigators who enter degree and residency completion dates will be notified of their ESI status by email.
Career stage of Early Stage Investigators (ESIs) will be considered during review and award selection.
Process to extend ESI stage for legitimate reasons (active military duty, medical concerns, disability, family care responsibilities, natural disasters, extended periods of clinical training, etc.) established.
See http://grants.nih.gov/grants/guide/notice-files/NOT-OD-09-103.html and http://grants.nih.gov/grants/guide/notice-files/NOT-OD-09-034.html.
More at: http://grants.nih.gov/grants/guide/notice-files/NOT-OD-09-013.html
Revised NIH Parental Leave Policy for NRSA AwardsRevised NIH Parental Leave Policy for NRSA AwardsTrainees on institutional training grants and individual fellowships may receive stipends for up
to 60 calendar days (equivalent to 8 work weeks) for parental leave per year.
NRSA programs affected: F30, F31, F32, F33, T32, T34, T35 and NRSA portion of T90 awards.
Applies to adoption or birth of a child when those in comparable training positions at the grantee organization have access to this level of paid parental leave.
Either parent is eligible.
The use of parental leave must be approved by the training Program Director.
More at: http://grants.nih.gov/grants/guide/notice-files/NOT-OD-08-064.html
Revised Policy on Concurrent Support from K Awards and Research GrantsRevised Policy on Concurrent Support from K Awards and Research Grants
“Recipients of mentored career development (K) awards may reduce effort on their K award in its final two years when they successfully compete for a peer-reviewed research grant from any Federal agency.”
Effort may be reduced to no less than 6 person-months (or 50% full-time professional effort) and replaced with effort from the research award so the total research effort commitment remains at 9 person-months (75% effort).
K awardee must be one of the named PIs on a competing research grant application or sub-project director on multi-component research or center grant or cooperative agreement.
More at: http://grants.nih.gov/grants/guide/notice-files/NOT-OD-08-065.html
Additional New Policies on “K” Career Development AwardsAdditional New Policies on “K” Career Development Awards
K recipients may request NIH permission to reduce their full-time appointment to less than full-time (but not less than 75%) for a period not to exceed 12 continuous months during the K award period. Option available only after K award is issued.
Under certain circumstances (accommodating parental leave, child care, medical conditions, or disability, but not job opportunities, clinical practice/training, or joint appointments.) K awardees may request NIH permission to reduce professional effort to less than 75% (but over 50%) for up to 12 continuous months.
A temporary career development experience at another institution for 3 months or less allowable without NIH permission.
A leave of absence may be taken without award support, but may not exceed 12 months.
More at: http://grants.nih.gov/grants/guide/notice-files/NOT-OD-09-036.html
Implementation UpdateImplementation Update Improve Scoring – Implementation in May, 2009.
~ Applications will receive an overall score from each panel member from 1-9; scores will be averaged and multiplied by 10. Thus priority scores will range between 10-90.
~ Priority scores will be percentiled against an appropriate base and reported in whole numbers.
Improve Critiques – Implementation in May, 2009.
~ Reviewer critiques will be compiled into a summary statement that will be shorter and more focused than currently due to standardized organization and reporting of strengths and weaknesses.
~ ALL applications (including streamlined applications) will receive feedback.
More at: http://grants.nih.gov/grants/guide/notice-files/NOT-OD-09-024.html
Public Access PolicyPublic Access Policy Compliance mandated by Public Law 110-161 via Omnibus Appropriations Act of
2009 The policy requires investigators who are funded by NIH to submit their final peer-
reviewed manuscripts to PubMed Central. Applicable to:
~ Peer-reviewed articles,~ Accepted for publication on or after 4/7/08, and~ Arising from direct grant or contract funds active in FY 2008, and beyond.
Full-text articles to be made publicly available on NLM’s PubMed Central no later than 12 months after date of publication
NIH is going to start cracking down on the policy and may take one or more enforcement actions depending on the severity and duration of non-compliance.
For questions regarding the policy please contact Cathy Sarli at 362-7865
More at: http://grants.nih.gov/grants/guide/notice-files/NOT-OD-08-119.html
Registration of Clinical TrialsRegistration of Clinical Trials
The FDA Amendments Act (P.L. 110-85) mandates registration and results reporting at ClinicalTrials.gov by sponsors of applicable clinical trials.
Expansion of existing ClinicalTrials.gov registry.
Includes Phase II-IV clinical trials of drugs and devices subject to FDA regulation.
Increased number of data elements that must be submitted.
Not limited to trials for serious or life threatening diseases.
Competing applications and progress reports grants with NIH-funded trials must include a certification of submission.
NIH encourages registration in ClinicalTrials.gov of ALL clinical research trials funded by NIH, whether required under the law or not.
More at: http://grants.nih.gov/grants/guide/notice-files/NOT-OD-08-023.html
Federal Funding Accountability and Transparency Act (FFATA)Federal Funding Accountability and Transparency Act (FFATA)
Public Law 109-282 requires information on every grant, including 1) the amount, 2) descriptive purpose of the grant, and 3) name and location of recipient of primary performance location.
Prepare for potential increased attention and scrutiny when data is made publicly available.
NIH is actively involved with a variety of Federal-wide committees to implement the act and is tailoring processes to meet its requirements.
FFATA has required form changes in the 424 (R&R) and PHS 398 to capture performance site information. – Stay Tuned!
Requires reporting on all subawards over $25,000. Pilot system for collecting currently in development – Stay Tuned!
More at: www.FederalSpending.gov
FCOI Summary of Reporting RequirementsFCOI Summary of Reporting Requirements
At the time of application: Investigators must submit known significant financial interests to the institution.
Prior to the expenditure of funds: The institution must report a financial conflict of interest to the NIH and assure that it has been managed, reduced, or eliminated.
FCOI identified after the initial report: The institution must report within 60 days of identification and assure that it has been managed, reduced, or eliminated.
More at: http://grants.nih.gov/grants/guide/notice-files/NOT-OD-05-013.html
FY 2009 OIG Audit Work Plan Selected HighlightsFY 2009 OIG Audit Work Plan Selected Highlights Colleges’ and Universities’ Compliance with Cost Principles
~ Cost transfers, effort reporting, and other areas
Use of Data and Safety Monitoring Boards in Clinical Trials
NIH Monitoring of Extramural Conflicts of Interest~ How NIH monitors extramural grantees’ FCOI and the effectiveness of NIH’s oversight
Grantee Management of Financial Conflicts of Interest in Research Funded by the NIH~ Monitoring of FCOIs, nature of FCOIs, and how FCOIs are managed (for FCOIs
reported to NIH in FY 2006)
FY 2009 Work Plan: http://oig.hhs.gov/publications/workplan.asp
Adobe Application Forms and Electronic Submission
Changes to electronic applications are on the wayLearn Changes to electronic applications are on the wayLearn how this affectshow this affects YOU YOU
Sample Changes to Application FormsSample Changes to Application Forms R&R Senior/Key Person Profile
~ Added Degree Type and Year (will allow NIH to remove Degree fields from PHS 398 Cover Pg Supplement)
R&R Project/Performance Site Location(s)~ Moved Congressional District data from R&R Cover Component~ Added DUNS Number field
PHS 398 Checklist ~ Added Disclosure Permission Statement
R&R Other Project Information ~ Re-ordered and revised Human Subjects fields ~ Revised fields on Environmental Impact~ Added field for impact on Historical Places
More at: http://grants.nih.gov/grants/forms.htm
PHS398 Changes
FFATA Changes
SF424 (R&R) Renewal
FutureFuture Transitions to Electronic Submission with Adobe Forms Transitions to Electronic Submission with Adobe Forms
80%
2%
7%
5%6%
Electronic
Training (T)
Fellowship (F)
Career Dev. (K)
Complex
• Fellowship (F): August 8, 2009 (tentative)• Training (T): September 25, 2009• Complex: TBD
Timeline is subject to change due to Grants.gov form development delays
More at: http://era.nih.gov/ElectronicReceipt/strategy_timeline.htm
Reminder: Avoid Common eSubmission ErrorsReminder: Avoid Common eSubmission Errors Use PDF format for text attachments and do not embed
movies or other materials in PDF attachments.
R&R Senior/Key Person Profile(s) form ~ Include eRA Commons Username in the ‘Credential, e.g., agency login’ field for all
individuals assigned a PD/PI role.~ Include the Organization Name for all Senior/Key Persons listed.
R&R Budget form - Senior/Key Person effort must be greater than zero.
Clicking ‘Submit’ is not the last step. Remember. . . if you can’t view it in Commons, we can’t review it
More at: http://era.nih.gov/ElectronicReceipt/avoiding_errors.htm
X-TrainX-Train X-Train is a new system to improve the administration of NIH Training
Grants.~ Allows PIs and staff to electronically submit appointment forms and
termination notices ~ Allows institutional staff to track status and timing of appointment
actions~ Will be available through eRA Commons
Pilot testing expanded to all FDP institutions in June, 2008.
Full production release expected in 2009.
More at : http://grants.nih.gov/grants/guide/notice-files/NOT-OD-08-081.html
Profile MaintenanceProfile Maintenance PIs have an obligation to keep information in their Personal Profile current and need
to update it regularly
Profile data used in other electronic processes (e.g., Summary Statements, eNotifications)
~ Degrees
~ Position Titles
~ Addresses - e-mail & postal
Especially critical for early stage investigators
Summary of Helpful NIH Web PagesSummary of Helpful NIH Web Pages NIH Searchable Database of RFAs, PAs, and Guide Notices
http://grants.nih.gov/grants/guide/index.html
NIH Grants Policy Statement (Rev. 12/03) http://grants.nih.gov/grants/policy/nihgps_2003/index.htm
NIH Extramural Nexus – Monthly newsletter (previously bimonthly) for the extramural communityhttp://grants.nih.gov/grants/nexus.htm
CRISP database - Search to analyze an Institute’s portfolio of funded projects, research areas, and more http://report.nih.gov/crisp.aspx
Grant Application Basics http://grants.nih.gov/grants/grant_basics.htm
OER Outreach Web Pagehttp://grants.nih.gov/grants/outreach.htm
NIH Regional Seminars on Program Funding and Grants AdministrationNIH Regional Seminars on Program Funding and Grants Administration
Yearly seminars to educate research administrators, investigators new to NIH, and trainees.
Due to the popularity of these seminars and availability of space - Early Registration is Highly Recommended!
Seminar and Registration Information: http://grants.nih.gov/grants/seminars.htm
Interested in hosting? Contact us!
More at: http://grants.nih.gov/grants/seminars.htm
NIH OER Listserv Addresses and InstructionsNIH OER Listserv Addresses and Instructions Office of Biotechnology Activities (OBA):
~ https://list.nih.gov/archives/oba_news.html
Office of Human Research Protections (OHRP): ~ http://www.hhs.gov/ohrp/news/distributionlist.html
Office of Laboratory Animal Welfare (OLAW):~ http://grants.nih.gov/grants/olaw/references/list.htm
eSubmission: ~ http://era.nih.gov/ElectronicReceipt/listserv.htm~ Separate listservs available for scientists and administrators
NIH Guide for Grants and Contracts:~ http://grants.nih.gov/grants/guide/listserv.htm~ The official publication for NIH medical and behavioral research Grant Policies, Guidelines
and Funding Opportunities
53
Selecting the “Next Reviewer” in eRA for eSNAPSSelecting the “Next Reviewer” in eRA for eSNAPS
NIH had previously approved of WU using the generic account of “WUSM App” as an SO account for submitting eSNAPs, but they have since changed their minds.
Effective June 1, 2009, please revert to the previous practice of listing your Grant Analyst as the “Next Reveiwer” in eRA for eSNAP applications.
54
Selecting the “Next Reviewer” in eRA for eSNAPSSelecting the “Next Reviewer” in eRA for eSNAPS
Go to for the latest instructions
www.grantsandcontracts.com
Under Application Process
See eSNAP procedure
Submission StatisticsSubmission Statistics
55
Month FY08 FY09 DELTA % Change
Mar 245 291 46 18%
Apr 215 654 439 204%
May 245 118* n/a n/a
*As of May 12
Competitive Revisions (supplements) submitted for 4/21/09 = 44RC1’s submitted for 4/27/09 = 174
58
Barnes Jewish Hospital Foundation F&ABarnes Jewish Hospital Foundation F&A
The BJHF Guidelines read as follows regarding 0% F&A:
“Grants funded from BJH Foundation Endowed Chairs and Special Requests (e.g. recruitment funds) as approved by WUSM will not receive indirect costs.”
In the past G&C was given the authority to approve “recruitment”, “start-up”, “special request” and “per so-and-so at BJHF s this should be 0%”. It is now being dictated that G&C should not approve any justification other than “endowed chair” for 0% F&A. From this point forward, the Dean wants to review all requests for less than BJHF’s published rates.
59
Any F&A rate that deviates from the above rates is subject to the F&A Waiver Process (Developed Nov. 2006), as follows:
F&A Waiver Process (PI/Dept. submits F&A letter to reduce or waive F&A)
Budget can go out with reduced F&A rate or no F&A rate (as decided by PI)
PDS doc. -> Should reflect reduced F&A rate or 0%. An over-ride to the F&A is needed.
PDS doc. -> Dept. should enter comment, “Dept. agrees to submit overhead reduction or waiver request to Dean. If the Dean does not approve the waiver, the dept. agrees to cover costs (i.e., cost sharing) to cover applicable F&A OR; dept. agrees that Direct Costs will be cut to cover associated F&A
Hard Copy ->Should reflect reduced F&A rate or 0%
Barnes Jewish Hospital Foundation F&A (cont.)Barnes Jewish Hospital Foundation F&A (cont.)
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Barnes Jewish Hospital Foundation F&A (cont.)Barnes Jewish Hospital Foundation F&A (cont.)
Notes:
This processes apply to any year of an BJHF award (e.g. year one and/or any subsequent years regardless of whether it is competitive or non-competitive).
This processes apply to Notice of Awards that are issued at 0% F&A, but do not site “endowed chair” as the reason for 0% F&A.
Setup of award could be delayed If F&A issue has not been resolved. Reminder: F&A reduction or waivers should be sent to G&C first. G&C will then forward the waiver to the Dean.
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““NEW” Human/Animal Approval Verification ProcessNEW” Human/Animal Approval Verification Process
Scenario A Human/Animal approval verification needs to be sent with an application, or JIT that will have a separate signature (i.e. face page, cover letter, etc.).The human/animal approval should be sent with the application. It will not be necessary for G&C to sign the approval as signature on the Face Page, or cover letter applies to everything in the packet.
Scenario BThe agency has a form that should be utilized for informing the agency of an animal approval verification (e.g. March of Dimes form). Department should complete the form and submit to G&C with the applicable approval. G&C will sign the form (not the approval).
Scenario CThe agency does not have a form for sending human/animal approval verification.Department should submit the approval to G&C. G&C will stamp the actual approval with John’s information (John Michnowicz, Director, Grants & Contracts, Washington University, School of Medicine) and provide signature on the approval.
Note: In cases where the PI, title, or funding source do not match the application, the department should provide a “Certification of Grant/Study Correspondence” form, but G&C would still sign off on the applicable approval that was provided.